Package 84549-071-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-071-10
Digits Only 8454907110
Product NDC 84549-071
Product ID 84549-071_3a388817-cca6-540d-e063-6294a90a6b35
Description

1 mL in 1 VIAL (84549-071-10)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "3a388817-cca6-540d-e063-6294a90a6b35", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["3856ea66-29b8-8fc2-e063-6394a90ac33a"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (84549-071-10)", "package_ndc": "84549-071-10", "marketing_start_date": "20250827"}], "brand_name": "Naloxone Hydrochloride", "product_id": "84549-071_3a388817-cca6-540d-e063-6294a90a6b35", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "84549-071", "generic_name": "Naloxone Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA207633", "marketing_category": "ANDA", "marketing_start_date": "20170808", "listing_expiration_date": "20261231"}